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Neutral acylation (protection) of the indole nitrogen: A simple synthesis of indole-1-carboxylates, indole-1-thiocarboxylates and indole-1-carboxamides

โœ Scribed by John E. Macor; Alison Cuff; Lyndon Cornelius

Publisher
Elsevier Science
Year
1999
Tongue
French
Weight
187 KB
Volume
40
Category
Article
ISSN
0040-4039

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โœฆ Synopsis

A simple synthesis of indole-l-carboxylates, indole-l-thiocarboxylates and indole-l-carboxamides (1) under neutral conditions is described.

๐Ÿ“œ SIMILAR VOLUMES

ChemInform Abstract: Neutral Acylation (
ChemInform Abstract: Neutral Acylation (Protection) of the Indole Nitrogen: A Simple Synthesis of Indole-1-carboxylates, Indole-1-thiocarboxylates and Indole-1-carboxamides.
โœ John E. Macor; Alison Cuff; Lyndon Cornelius ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 29 KB ๐Ÿ‘ 2 views

1999 indole derivatives, isoindole derivatives indole derivatives, isoindole derivatives R 0140 ## 27 -136 Neutral Acylation (Protection) of the Indole Nitrogen: A Simple Synthesis of Indole-1-carboxylates, Indole-1-thiocarboxylates and Indole-1-carboxamides. -The conversion of N-unsubstituted in

Divergent synthesis of isoindolo[2,1-a]i
Divergent synthesis of isoindolo[2,1-a]indole and indolo[1,2-a]indole through copper-catalysed C- and N-arylations
โœ Nekane Barbero; Raul SanMartin; Esther Domรญnguez ๐Ÿ“‚ Article ๐Ÿ“… 2009 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 292 KB

A simple and efficient synthetic route to both isoindolo[2,1-a]indole and its structural isomer indolo[1,2a]indole skeletons is presented. The key steps of the strategy are based on copper-catalysed C aryl -C and C aryl -N bond formation reactions, respectively. Moreover, we report the first copper-